Tet1 is dispensable for maintaining pluripotency and its loss is compatible with embryonic and postnatal development

Cell Stem Cell

Volumn 9, Issue 2, 2011, Pages 166-175

  Dawlaty, Meelad M ^a   Ganz, Kibibi ^a   Powell, Benjamin E ^a   Hu, Yueh Chiang ^a   Markoulaki, Styliani ^a   Cheng, Albert W ^a,b   Gao, Qing ^a   Kim, Jongpil ^a   Choi, Sang Woon ^c   Page, David C ^a,b,d   Jaenisch, Rudolf ^a,b  

^a WHITEHEAD INSTITUTE FOR BIOMEDICAL RESEARCH   (United States)

^b MASSACHUSETTS INSTITUTE OF TECHNOLOGY   (United States)

^c TUFTS UNIVERSITY   (United States)

^d HOWARD HUGHES MEDICAL INSTITUTE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

5 HYDROXYMETHYLCYTOSINE; ONCOPROTEIN; PROTEIN TEN ELEVEN TRANSLOCATION 1; UNCLASSIFIED DRUG;

ANIMAL CELL; ANIMAL EXPERIMENT; ARTICLE; BODY SIZE; CELL DIFFERENTIATION; DNA METHYLATION; EMBRYO DEVELOPMENT; EMBRYONIC STEM CELL; FEMALE; GENE EXPRESSION; MALE; MOUSE; NONHUMAN; NUCLEOTIDE SEQUENCE; POSTNATAL DEVELOPMENT; PRIORITY JOURNAL; TETRAPLOIDY;

ANIMALS; ANIMALS, NEWBORN; BODY SIZE; CYTOSINE; DNA METHYLATION; DNA-BINDING PROTEINS; EMBRYO, MAMMALIAN; EMBRYONIC DEVELOPMENT; EMBRYONIC STEM CELLS; FEMALE; FERTILITY; GENE EXPRESSION REGULATION, DEVELOPMENTAL; GENE KNOCKOUT TECHNIQUES; GENETIC COMPLEMENTATION TEST; MICE; MICE, INBRED C57BL; PLURIPOTENT STEM CELLS; PROTO-ONCOGENE PROTEINS; TETRAPLOIDY;

MUS;

EID: 79961139741     PISSN: 19345909     EISSN: 18759777     Source Type: Journal    
DOI: 10.1016/j.stem.2011.07.010     Document Type: Article

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